Metabolic Fuel for Epigenetic: Nuclear Production Meets Local Consumption

被引:20
作者
Boon, Ruben [1 ,2 ,3 ]
机构
[1] Harvard Med Sch, Massachusetts Gen Hosp, Canc Ctr, Boston, MA 02115 USA
[2] Broad Inst Harvard & MIT, Cambridge, MA 02142 USA
[3] Katholieke Univ Leuven, Dept Human Genet, Lab Funct Epigenet, Leuven, Belgium
关键词
nuclear metabolism; epigenetics; liquid-liquid phase separation (LLPS); compartmentalization; chromatin; PYRUVATE-DEHYDROGENASE COMPLEX; HISTONE DEACETYLASE ACTIVITY; PROMOTES GENE-TRANSCRIPTION; ACETYL-COA; TUMOR-SUPPRESSOR; PHASE-SEPARATION; DNA-REPAIR; ACYL-COA; SIRT6; CHROMATIN;
D O I
10.3389/fgene.2021.768996
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Epigenetic modifications are responsible for finetuning gene expression profiles to the needs of cells, tissues, and organisms. To rapidly respond to environmental changes, the activity of chromatin modifiers critically depends on the concentration of a handful of metabolites that act as substrates and co-factors. In this way, these enzymes act as metabolic sensors that directly link gene expression to metabolic states. Although metabolites can easily diffuse through the nuclear pore, molecular mechanisms must be in place to regulate epigenetic marker deposition in specific nuclear subdomains or even on single loci. In this review, I explore the possible subcellular sites of metabolite production that influence the epigenome. From the relationship between cytoplasmic metabolism and nuclear metabolite deposition, I converse to the description of a compartmentalized nuclear metabolism. Last, I elaborate on the possibility of metabolic enzymes to operate in phase-separated nuclear microdomains formed by multienzyme and chromatin-bound protein complexes.
引用
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页数:15
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